Abstract

Chronic rhinosinusitis is the foremost manifestation in adult patients with primary ciliary dyskinesia (PCD). We present a retrospective series of 41 adult patients with a confirmed diagnosis of PCD followed in our reference centers. As part of the diagnostic work up in our centers, sinus computed tomography scans (CTs) are systematically performed. All patients also undergo a sampling of purulent secretions sampled from the middle meatus under endoscopic view for bacteriological analysis. In our series, CT opacities were consistent in all the patients, as well as mainly partial and located in ethmoid cells (100% of patients) and in maxillary sinuses (85.4% of patients), and stayed stable over time. In the 31 patients who had purulent secretions, bacteriological culture showed at least one bacterium in 83.9% (n = 26). There was no significant difference in positive cultures for Pseudomonas aeruginosa in patients >40 years old versus those <40 (p = 0.17; Fisher). Surgical management was performed in only 19% of patients in order to improve sinonasal mechanical drainage. Our data support the hypothesis that the sinuses can be considered as a bacterial reservoir. From this retrospective study, we have introduced several changes into our routine clinical practice in our reference centers. Based on our analyses, medical and surgical treatments benefit from incorporating bacteriological information and sinonasal symptoms much more than CT scan evaluation alone. All patients now undergo systematically an annual simultaneous bacteriological sampling of the middle meatus and sputum to follow the relationship between ENT and lung disease and to help to antibiotic therapy strategy.

Highlights

  • Primary ciliary dyskinesia (PCD) is an autosomal recessive genetic disorder leading to structural and/or functional abnormalities of the cilia

  • We have already published that Chronic rhinosinusitis (CRS) is present in 94.8% of adult patients with primary ciliary dyskinesia (PCD), and nasal polyps are reported in 15% to 56% [1,2]

  • A specific evaluation of quality life focusing on nasal symptoms: Sinonasal Outcome Test 22 (SNOT-22) is performed in our centers in order to evaluate the impact of our treatments for rhinosinusitis

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Summary

Introduction

Primary ciliary dyskinesia (PCD) is an autosomal recessive genetic disorder leading to structural and/or functional abnormalities of the cilia. In a recent state-of-the-art study [2], Honoré et al underlined the fact that the management of PCD remains poorly defined and should be performed by specialized centers in order to standardize follow-up and improve patient outcome. Chronic rhinosinusitis (CRS) in patients with PCD is at the forefront of the disease presentation in adults [3], but it has been poorly studied [4].

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